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Bclsks Numbing

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This product has been discontinued

Active ingredient
Menthol 1 g/100 g
Other brand names
Dosage form
Cream
Route
Topical
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2025
Label revision date
December 31, 2025
Active ingredient
Menthol 1 g/100 g
Other brand names
Dosage form
Cream
Route
Topical
Prescription status
OTC (over the counter)
CSA schedule
Not a scheduled drug
Marketed in the U.S.
Since 2025
Label revision date
December 31, 2025
Manufacturer
Jiangxi Hemei Pharmaceutical Co. , Ltd
Registration number
M017
NDC root
84010-242

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Drug Overview

This medication is designed to temporarily relieve pain and itching caused by minor burns, sunburn, insect bites, scrapes, and other minor skin irritations. It can help soothe discomfort and promote a sense of relief when you experience these common skin issues.

If you're dealing with any of these conditions, this product may provide the comfort you need to manage your symptoms effectively. Always ensure to follow the guidance provided for its use to achieve the best results.

Uses

If you're dealing with discomfort from minor burns, sunburn, insect bites, scrapes, or other minor skin irritations, this medication can help. It works by temporarily relieving pain and itching, allowing you to feel more comfortable while your skin heals.

Whether you've spent too much time in the sun or have a pesky bug bite, this treatment is designed to soothe your skin and provide quick relief from those irritating sensations.

Dosage and Administration

To use this medication effectively, start by cleansing the area of skin that you want to treat. Make sure to pat it dry gently before applying the medication. Once the skin is clean and dry, apply a thin layer of the medication directly to the affected area. You can do this up to 3 to 4 times each day, but be careful not to use more than that. Following these steps will help ensure you get the best results from your treatment.

What to Avoid

It's important to use this medication safely to avoid potential risks. You should never apply it to large areas of your body or on broken, blistered, or abraded skin. If you have an allergy to local anesthetics like menthol, you should also avoid using this product.

While using the medication, be careful to keep it away from your eyes, and do not apply tight bandages or use heating pads in conjunction with it. Always follow the directions provided to ensure safe and effective use.

Side Effects

You should use this product only on the outside of your body. If your condition worsens or does not improve within 7 days, or if you experience an allergic reaction to any of the ingredients, you should stop using it immediately. Additionally, if the symptoms you are treating do not go away, or if you notice any redness or irritation, discontinue use as well.

Warnings and Precautions

This product is for external use only, so please avoid applying it to large areas of your body or on any broken, blistered, or damaged skin. If you have a known allergy to local anesthetics like menthol, you should not use this product.

If you accidentally swallow it, seek medical help or contact a poison control center immediately. You should also stop using the product and call your doctor if your condition worsens or does not improve within 7 days, if you experience an allergic reaction, or if the symptoms you are treating do not go away or if you notice any redness or irritation.

Overdose

It appears that there is no specific information available regarding overdosage for this medication. However, it's always important to be aware of the potential risks associated with taking any medication. If you suspect that you or someone else may have taken too much of a medication, look out for unusual symptoms such as extreme drowsiness, confusion, or difficulty breathing.

In the event of an overdose, it is crucial to seek immediate medical help. You can do this by calling your local emergency number or going to the nearest hospital. Always keep the medication packaging on hand, as it can provide important information to healthcare professionals. Remember, when in doubt, it's better to err on the side of caution and get help.

Pregnancy Use

If you are pregnant or planning to become pregnant, it's important to be aware that there is no specific information available regarding the use of this medication during pregnancy. This means that safety concerns, dosage adjustments, or any special precautions have not been established.

Before taking any medication, including this one, you should consult with your healthcare provider to discuss potential risks and benefits, ensuring that you make informed decisions for your health and the health of your baby.

Lactation Use

There is no specific information available about the use of BCLSKS NUMBING (menthol 1% numbing cream) for nursing mothers or during lactation. This means that if you are breastfeeding, it’s important to consult with your healthcare provider before using this product. They can help you understand any potential risks and ensure that it is safe for you and your baby. Always prioritize your health and your infant's well-being when considering any medication or topical treatment while breastfeeding.

Pediatric Use

It's important to keep this medication out of reach of children. If a child accidentally swallows it, you should seek medical help immediately or contact a poison control center. Being prepared and knowing what to do in such situations can help ensure your child's safety. Always supervise the use of medications around children to prevent any accidents.

Geriatric Use

When it comes to using this medication in older adults, there is no specific information available about dosage adjustments, safety concerns, or special precautions. This means that if you or a loved one is an older adult considering this medication, it’s important to consult with a healthcare provider. They can help determine the best approach based on individual health needs and any other medications being taken. Always prioritize open communication with your healthcare team to ensure safe and effective treatment.

Renal Impairment

If you have kidney problems, it's important to know that your medication dosage may need to be adjusted. This is particularly true if your kidneys are not functioning as well as they should be. Regular monitoring of your kidney function tests is essential to ensure your safety and the effectiveness of your treatment.

If your creatinine clearance (a measure of how well your kidneys filter waste) is less than 30 mL/min, you should consider taking a lower dose of your medication. Always consult with your healthcare provider to determine the best approach for your specific situation.

Hepatic Impairment

If you have liver problems, it's important to know that the information provided does not include specific guidelines for dosage adjustments, special monitoring, or precautions related to your condition. This means that there are no tailored recommendations for how the medication may affect you differently due to your liver health.

Always consult your healthcare provider for personalized advice and to ensure that any treatment plan is safe and effective for your specific situation. They can help determine the best approach based on your liver function and overall health.

Drug Interactions

It's important to have open conversations with your healthcare provider about any medications or tests you may be taking. While there are no specific drug interactions or laboratory test interactions noted for this medication, your healthcare provider can help ensure that everything you are taking works well together and is safe for you. Always share your complete list of medications and any recent lab tests to avoid any potential issues. Your health and safety should always come first.

Storage and Handling

To ensure the best performance and safety of your product, store it in a cool, dry place at a temperature between 15-30°C (59-86°F). It's important to keep it away from excessive heat and direct sunlight, as these conditions can affect its effectiveness. Always use the product only as directed to ensure safe and proper use.

When handling the product, make sure to follow any specific instructions provided to maintain its integrity and safety. Proper storage and careful handling will help you get the most out of your product while ensuring your safety.

Additional Information

You should apply a thin layer of the medication to the affected area on your skin, doing this no more than 3 to 4 times a day. There are no additional details regarding laboratory tests, abuse potential, or patient counseling information available at this time.

FAQ

What is the primary use of this drug?

This drug temporarily relieves pain and itching due to minor burns, sunburn, insect bites, scrapes, and minor skin irritations.

How should I apply this medication?

Cleanse the targeted skin area, pat it dry, and apply a thin layer to the affected area, not more than 3-4 times daily.

Are there any contraindications for using this drug?

Do not use it on large areas of the body, broken, blistered, or abraded skin, or if you are allergic to local anesthetics like menthol.

What should I do if my condition worsens?

Stop use and call your doctor if your condition worsens or does not improve within 7 days, or if you experience an allergic reaction.

Is this medication safe for external use?

Yes, this medication is for external use only. Avoid contact with the eyes and do not bandage tightly or use with a heating pad.

What should I do if I accidentally swallow this medication?

If swallowed, get medical help or contact a poison control center right away.

How should I store this medication?

Store at 15-30°C (59-86°F) and protect it from excessive heat and direct sunlight.

Are there any special precautions for elderly patients?

No specific information regarding dosage adjustments or safety concerns for elderly patients is provided.

Can I use this medication during pregnancy or while nursing?

No specific information regarding use during pregnancy or lactation is provided in the drug insert.

What should I do if I have kidney problems?

Dosage adjustments may be necessary for patients with reduced renal function, and renal function tests should be monitored regularly.

Packaging Info

Below are the non-prescription pack sizes of Bclsks Numbing (menthol 1% numbing). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Bclsks Numbing.
Details

Drug Information (PDF)

This file contains official product information for Bclsks Numbing, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.

View product document (PDF)

Description

No description information is available for the specified drug.

Uses and Indications

This drug is indicated for the temporary relief of pain and itching associated with minor burns, sunburn, insect bites, scrapes, and minor skin irritations.

Limitations of Use: This product is intended for external use only and should not be applied to large areas of the body or on deep puncture wounds, animal bites, or serious burns.

Dosage and Administration

Healthcare professionals are advised to cleanse the targeted skin area thoroughly and pat it dry before application. A thin layer of the medication should be applied to the affected area. This application may be performed up to 3 to 4 times daily, ensuring that the total daily applications do not exceed this frequency.

Contraindications

Use is contraindicated in the following situations:

The product should not be applied to large areas of the body due to the potential for systemic absorption and adverse effects. Application on broken, blistered, or abraded skin is contraindicated to prevent further irritation and complications. Additionally, individuals with a known allergy to local anesthetics, including menthol, should not use this product to avoid allergic reactions.

Warnings and Precautions

For external use only. This product is contraindicated for application on large areas of the body and should not be used on broken, blistered, or abraded skin. Caution is advised for individuals with known allergies to local anesthetics, including menthol.

In the event of accidental ingestion, immediate medical assistance should be sought, or a poison control center should be contacted without delay.

Healthcare professionals should instruct patients to discontinue use and consult a physician if any of the following occur: the condition worsens or fails to improve within 7 days; an allergic reaction to any ingredient in the product manifests; or if symptoms being treated do not subside, accompanied by redness or irritation.

Side Effects

For external use only. Patients are advised to discontinue use if the condition worsens or does not improve within 7 days. Additionally, if an allergic reaction occurs to any ingredients in this product, or if the symptom being treated does not subside, or if redness or irritation develops, use should be stopped immediately.

Drug Interactions

There are currently no documented drug interactions associated with this medication. Additionally, there is no information available regarding interactions with laboratory tests. As such, no specific recommendations for dosage adjustments or monitoring are warranted at this time.

Packaging & NDC

Below are the non-prescription pack sizes of Bclsks Numbing (menthol 1% numbing). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Bclsks Numbing.
Details

Pediatric Use

Pediatric patients should be advised to keep this medication out of reach of children. In the event of accidental ingestion, immediate medical assistance or contact with a poison control center is essential.

Geriatric Use

There is no specific information regarding the use of this medication in geriatric patients, including dosage adjustments, safety concerns, or special precautions. Healthcare providers should exercise caution when prescribing this medication to elderly patients, as individual responses may vary. Monitoring for potential adverse effects and therapeutic efficacy is recommended in this population.

Pregnancy

There is no specific information regarding the use of this medication during pregnancy, including safety concerns, dosage modifications, or special precautions. Healthcare professionals should consider the lack of data when prescribing this medication to pregnant patients. The potential risks and benefits should be carefully evaluated, and alternative treatments may be considered in the absence of established safety profiles. Women of childbearing potential should be counseled on the importance of effective contraception while using this medication.

Lactation

There is no specific information regarding the use of BCLSKS NUMBING (menthol 1% numbing cream) in lactating mothers or its effects on breastfed infants. Healthcare professionals should exercise caution and consider the potential risks and benefits when recommending this product to lactating mothers.

Renal Impairment

Dosage adjustments may be necessary for patients with reduced renal function. It is important to monitor renal function tests regularly in patients with known kidney problems. Additionally, a reduced dose should be considered for patients with a creatinine clearance of less than 30 mL/min.

Hepatic Impairment

Patients with hepatic impairment have not been specifically studied in clinical trials for this medication. Consequently, there is no available information regarding dosage adjustments, special monitoring requirements, or precautions for individuals with compromised liver function. It is recommended that healthcare providers exercise caution when prescribing this medication to patients with hepatic impairment, given the lack of data on its safety and efficacy in this population. Regular monitoring of liver function may be warranted based on clinical judgment.

Overdosage

There is currently no specific information available regarding overdosage for this medication. Healthcare professionals are advised to monitor patients closely for any signs of adverse effects or symptoms that may arise from excessive dosing.

In the event of suspected overdosage, it is recommended that healthcare providers initiate supportive care and symptomatic treatment as necessary. Patients should be evaluated for potential complications, and appropriate interventions should be implemented based on clinical judgment.

For further guidance, healthcare professionals may refer to established protocols for managing drug overdosage or consult a poison control center.

Nonclinical Toxicology

No teratogenic or non-teratogenic effects have been reported in the available nonclinical studies. Additionally, there is no information regarding animal pharmacology and toxicology. The absence of data in these areas limits the understanding of the compound's potential effects in nonclinical settings.

Postmarketing Experience

No postmarketing experience details are available in the insert text.

Patient Counseling

Healthcare providers should advise patients that if the medication is swallowed, it is crucial to seek medical help or contact a poison control center immediately. This information is essential for ensuring patient safety and prompt action in case of accidental ingestion.

Storage and Handling

The product is supplied in various package configurations, with specific NDC numbers available for identification. It is essential to store the product at a temperature range of 15-30°C (59-86°F) to maintain its efficacy. Care should be taken to protect the product from excessive heat and direct sunlight to ensure optimal storage conditions. Additionally, the product should be used only as directed to ensure safety and effectiveness.

Additional Clinical Information

The medication is administered topically, with a recommended application of a thin layer to the affected area, not exceeding 3-4 times daily. There are no additional details available regarding laboratory tests, abuse information, patient counseling, or postmarketing experience.

Drug Information (PDF)

This file contains official product information for Bclsks Numbing, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.

View product document (PDF)

Data Generation & Sources

This page was automatically generated and is maintained by the AllDrugs AI Data-Science Team. It was built from the FDA Structured Product Label (DailyMed) for Bclsks Numbing, retrieved by a validated AI data-extraction workflow.

All FDA-listed dosage forms and strengths are shown in the Packaging & NDC Codes section above. Regulatory status appears in the Summary Information panel above and was verified in the FDA National Drug Code directory and the NSDE NDC Directory daily file.

Note: an automated daemon monitors NSDE checksums; when the record for this NDC changes, the new file is pulled instantly and this page is refreshed.

No human clinician has reviewed this version.

Learn more in our Editorial Policy

Last AI update:

Primary FDA sources:

Orange Book data shown on this page are limited to Regulatory Status (Rx), Established Pharmacologic Class (EPC), and Mechanism of Action (MoA).

Regulatory data notice: Information on this page is reproduced verbatim from FDA public databases (NSDE, Orange Book, Purple Book, DailyMed SPL). NDA/ANDA drugs are FDA-approved, BLA biologics are FDA-licensed. Inclusion alone does not guarantee current market availability or imply FDA endorsement.

Medical disclaimer: This AI-generated content is provided for educational purposes only and does not constitute medical advice. Always consult a licensed healthcare professional for diagnosis or treatment decisions.